Composite material having absorbable and non-absorbable components for use with mammalian tissue

ABSTRACT

The invention is a composite material of two or more biocompatible polymers, at least one of which is polytetrafluoroethylene (PTFE) and one of which is a bioabsorbable polymer. The nonabsorbable PTFE is used in the composite as a reinforcing binder. The reinforcing binder is a network of unsintered, interconnected micro-fibers which are formed, for example, by blending with a thermoplastic polymer vehicle, such as polymethylmethacrylate which is subsequently extracted. The bioabsorbable component is contained within the structure of the PTFE microfibrils. This composite is useful in the repair of mammalian tissue where tissue ingrowth and permenant support is required.

This is a continuation of co-pending application Ser. No. 07/475,564,filed on Feb. 6, 1990, now abandoned.

BACKGROUND AND SUMMARY OF THE INVENTION

This invention relates to a composite of two or more biocompatiblepolymers, at least one of which is polytetrafluoroethylene (PTFE) andthe other component being a bioabsorbable polymer. The nonabsorbablePTFE is used in the composite as a reinforcing binder. The reinforcingbinder is a network of unsintered, interconnected microfibers. Themicrofibers can be formed, for example, by blending with a thermoplasticpolymer vehicle, such as polymethylmethacrylate. The bioabsorbablepolymer component can be present in the form of a particulate fillercontained within the PTFE microfibrillar structure. The bioabsorbableparticulate component can be micropulverized and could be, for example,polyglycolic acid (PGA), polylactic acid (PLA), a homo- or copolymer oftrimethylene carbonate (TMC), and blends of the same or similarpolymers. The polymethylmethacrylate is subsequently extracted with asuitable solvent. The resulting microporous structure has a tortuousporosity.

Alternatively, the bioabsorbable polymer can serve as the thermoplasticvehicle during the PTFE fibrillation process thus resulting in anonporous reinforced composite structure. The bioabsorbable polymervehicle component could be a copolymer of polyglycolic acid andtrimethylene carbonate (GLY/TMC) or other bioabsorbable thermoplastic.

The composite described in this application may be useful in manybiomedical applications, such as a tissue, hernia, or ligament repairdevice, a burn or wound dressing, a pledget, a drug delivery system anda tubular article, for example a vascular graft. The bioabsorbablecomponent enhances tissue ingrowth within the fibrillar PTFE matrix. Thenonabsorbable microfibrillar PTFE matrix provides additional support,direction and strength to the natural tissue formation.

The composite polymer structure described in this invention is useful inbiomedical applications, such as in tissue repair, hernia repair,ligament repair, burn and wound dressing, pledgets, drug deliverysystems, vascular grafts, etc. The bioabsorbable component enhancestissue ingrowth within the fibrillar PTFE matrix, which providesadditional support, direction and strength to the natural tissueformation.

An advantage of this invention is that since a thermoplastic vehicle isused to form the fibrillar PTFE matrix, it therefore can be extrudedinto many different shapes such as a rod, tube, tape, film, or otherintricate forms before extracting the thermoplastic.

Another advantage is that the PTFE is unsintered. Thus, the break downtemperature of known bioabsorbable polymers (e.g., less than about 250°C.) is avoided in the processing of the composite of this invention.

The completely fibrillated, unsintered polytetrofluoroethylene (PTFE)reinforcing binder of this invention has advantages over a prior artporous, sintered PTFE product. For a disclosure of a sintered PTFEproduct, see, e.g., "Fluorocarbons Available in New Fibrous, PorousConfigurations" published in Materials In Design Engineering, pages 5-7,May, 1965, which is incorporated herewith by reference.

Some of the advantages of this invention, in summary form, are asfollows. A filler can be added directly to the PTFE polymer withoutsubjecting it to the detrimental effects of the sintering temperature(approximately 325° F.) of PTFE. Also, a level as high as 97% fillercontent in the unsintered PTFE polymer can be achieved.

The prior art describes methods of preparation and nonbiological uses offibrillar PTFE. The nonbiological uses include electrochemicalapplications. See, e.g., U.S. Pat. Nos. 3,527,616; 3,407,249; and3,407,096 which are incorporated herein by reference.

A composite material for use with mammalian tissue has been invented.The composite material comprises:

a) an unsintered, microfibrillar, nonabsorbable biocompatible componentprepared from polytetrafluoroethylene, and from a polymer prepared fromone or more monomers selected from the group consisting of lactides,carbonates, oxalates and lactones, and optionally

c) a nonabsorbable, biocompatible thermoplastic component manufacturedfrom a polymer which is liquid at a temperature from about 150° to 200°C. and solid at ambient temperature, and which provides additionalintegrity to the unsintered component. In one embodiment, thebioabsorbable component is selected from the group consisting oflactides, carbonates and lactones. In a specific embodiment, thelactides are selected from the group consisting of glycolide and3,6-dimethyl-1,4-dioxane-2,5-dione; the carbonate is 1,3-dioxan-2-one;and the lactones are selected from the group consisting ofe-caprolactone and 1,4-dioxan-2-one. In another embodiment, thebioabsorbable component is manufactured from glycolide.

In combination with any of the above embodiments, other embodiments arethe bioabsorbable component enmeshed in the pores of the unsinteredcomponent; the composite material in the form of a sheet or a hollowtube; and the nonabsorbable, thermoplastic component beingpoly(ethylenevinylacetate).

Still another embodiment is wherein the nonabsorbbable, thermoplasticcomponent is enmeshed in the pores of the unsintered component. In aspecific embodiment, the nonabsorbable, thermoplastic component ispoly(ethylenevinyl acetate).

An alternative composite material for use with mammalian tissue has alsobeen invented. The alternative composite material comprises:

a) an unsintered, microfibrillar, non-absorbable biocompatible componentprepared from polytetrafluoroethylene, and

b) a particulate bioabsorbable component manufactured from a polymerprepared from one or more monomers selected from the group consisting oflactides, carbonates, oxalates and lactones, and optionally

c) a non-absorbable, biocompatible thermoplastic component manufacturedfrom a polymer which is liquid at a temperature from about 150° to 200°C. and solid at ambient temperature, and which provides additionalintegrity to the unsintered component. In one embodiment, theparticulate bioabsorbable component is selected from the groupconsisting of lactides, carbonates and lactones. In a specificembodiment, the lactides are selected from the group of glycolide and3,6-dimethyl-1,4-dioxan-2,5-dione; the carbonate is 1,3-dioxan-2-one;and the lactones are selected from the group consisting ofe-caprolactone and 1,4-dioxan-2-one. In another embodiment, thebioabsorbable component is manufactured from glycolide.

In combination with any of the above embodiments, other embodiments arethe particulate bioabsorbable component being micropulverized; thecomposite material in the form of a sheet or a hollow tube; and thenonabsorbable, thermoplastic component being poly(ethylene-vinylacetate).

Another alternative composite material for use with mammalian tissue hasalso been invented. The other alternative composite material comprises afirst part consisting of the two component and optional three componentcomposite material described above; and a second part affixed to atleast one side of the first part. The second part comprises abioabsorbable textile reinforcement component. The bioabsorbablereinforcement component is woven or knitted, and is manufactured fromthe same or a different polymer than the bioabsorbable component of thefirst part. In one embodiment, the bioabsorbable textile reinforcementcomponent is selected from the group consisting of lactides, carbonatesand lactones. In a specific embodiment, the lactides are selected fromthe group consisting of glycolide and 3,6-dimethyl-1,4-dioxan-2,5-dione; the carbonate is 3-dioxan-2-one; and the lactones areselected from the group consisting of e-caprolactone and1,4-dioxan-2-one. In another embodiment, the textile reinforcementmaterial is affixed to both sides of the first part. In a specificembodiment, the reinforcement material is laminated to the first part.

A drawing which describes the shape and/or geometrical configuration ofthe composite material is not necessary for an understanding of thisinvention. That is, any person skilled in the composite art will knowhow to manufacture and how to use the invention by reading thisspecification generally, and the examples specifically.

DESCRIPTION OF THE PREFERRED EMBODIMENT(S)

The material contains a fibrillated form of polytetrafluoroethylene(PTFE). It is processed without fusing the polymer at its sinteringtemperature (about 327° C.). It is a porous, membrane-like structurewhich is formed by mixing micro-particles of PTFE with a moltenthermoplastic polymer, such as polymethylmethacrylate. The thermoplasticblend is then formed into a film, or other configuration, and thethermoplastic phase is subsequently extracted with a suitable solvent.The resultant pliable unsintered, fibrillar PTFE has a tortuous porousstructure and is an excellent binder for many functional fillers.

One or more bioabsorbable polymers PGA fibers and/or micropulverized PGApowder can be incorporated into this porous PTFE fibrillar matrix. Thisbioabsorbable filler could enhance tissue ingrowth within its inherenttortuous porous structure. Therefore, it would be useful in ligamentreplacement and repair, membrane organ separators, burn or wounddressings, hernia repair, pericardial substitute etc.

Some changes could be made in the preparation of the film to reduce thefabricating temperatures below 100° C. This might include the use ofextractable polymers or other extractable vehicles other thanpolymethylmethacrylate. Also, the coagulation of the PTFE dispersion asdescribed in an article entitled, "Extrusion Properties of LubricatedResin From Coagulated Dispersion," (Industrial and EngineeringChemistry, Vol. 44, No. 8, August 1952, p. 1805) results in a viscousmass which might be milled and fabricated to form a completely fibrousPTFE sheet similar to those prepared by the present process. Otherimprovements in the process might include the use of water solublepolymers such as polyethylene oxide.

Various fillers can be incorporated into this film to levels as high as97%. As a filled, coated, or impregnated material, this unique porous,fibrous, unsintered PTFE offers a vast number of possibilities relatedto the combined properties of PTFE in this form with those of itsfiller, coating, etc. The use of additional extractable fillers tomodify the structure has been demonstrated (i.e. the postextraction ofcolloidal silica from catalyzed carbon filled electrode structures) asdisclosed in U.S. Pat. No. 3,527,616, which is incorporated herein byreference.

The fibrillar PTFE composite may be modified by combination with otherreinforcing agents, such as meshes, woven fabrics, knitted fabrics, etc.prepared from biocompatible polymers. Also, the PTFE (in themicropulverized or dispersion form before fibrillating) can beincorporated directly into a bioabsorbable thermoplastic polymer, suchas a homopolymer of polyglycolic acid (PGA), or a copolymer of PGA, e.g.one containing glycolic acid ester and trimethylene carbonate linkages(GLY/TMC), thus forming the microfibrillar structure in situ andeliminating the extractable thermoplastic vehicle. The fibrillar PTFEreinforced bioabsorbable polymer may also be extruded as a fiber for useas a suture, woven fabric, etc.

The thermoplastic vehicle may be removed such as by extraction with asuitable solvent. The remaining unsintered, fibrillar PTFE has atortuous, microporous structure which is an excellent binder at levelsas low as 1% for many functional fillers including bioabsorbablematerials such as PGA, GLY/TMC and polydioxanone. The novel feature ofthis invention is the addition of a bioabsorbable filler which enhancestissue ingrowth within the tortuous, microporous fibrillar structure ofthe non-absorbable PTFE, which acts as reinforcement for the new tissuegrowth.

This fibrous, unsintered PTFE may be used as a carrier, reinforcingagent, or binder for other polymeric materials, both thermoplastic orthermoset, incorporated directly or by post-impregnation to furtherenhance the composite structure and degree of porosity (from non-porousto highly porous).

As used in the examples below, the term Acrylite and Acrylite H-12 aretrademarks of American Cyanamide Company, N.J., U.S. for polymercompounds, such as a polymethylmethacrylate (herein abbreviated PMMA)compound. Also as used in the examples below, the term 30B susp. may bea condensation of the term Teflon™ 30B suspension, which term may be atrademark of E.I. duPont & Co., De., U.S. for polytetrafluoroethylene inan aqueous suspension.

EXAMPLES 1 TO 5

The Examples 1 and 4 to 7, respectively, of U.S. Pat. No. 3,407,249issued Oct. 22, 1968 to H. Landi and entitled "Porous, ExtensivelyFibrillated Polytetrafluoroethylene and Method of Preparing Same" areincorporated here by reference.

EXAMPLE 6

The Example 1 of U.S. Pat. No. 3,527,616 issued Sep. 8, 1970 to H. Landiand entitled "Electrodes for Free Electrolyte Fuel Cells" isincorporated here by reference.

EXAMPLE 7

The Example 1 of U.S. Pat. No. 3,407,096 issued Oct. 22, 1968 to H.Landi and entitled "Fuel Cell and Method for Preparing the Electrodes"is incorporated herein by reference.

EXAMPLE 8

A microporous bicomponent composite structure of fibrillated PTFEsemi-permeable membrane sheet containing high levels of micropulverizedPGA polymer is prepared as follows:

On a rubber mill are heated to about 160°-170° C. a molten blend of thefollowing ingredients, listed in order of addition, is mixed thoroughly:

    ______________________________________                                        Blend                                                                         No.     Components          Wt., q.                                           ______________________________________                                        1       Acrylite ™ H-12 Compound                                                                       200                                                       33.2 ml of PTFE In aqueous                                                                        30     PTFE                                               suspension - duPont 30B                                                       PGA micropulverized to about                                                                      170                                                       150 microns                                                           ______________________________________                                    

The micropulverized PGA powder is formed by grinding the polymer pelletsin a Fitzpatrick Mill mixed with dry ice to prevent overheating. Theresultant ground powder is sieved through a 100 mesh screen to recoverthe micropulverized powder of about 150 microns or less.

The blend was removed from the rubber mill in one uniform sheet. Whilethe blended sheet was still hot from the mill, it was cut into 8 piecesof approximately equal size to be used for compressing into thinnersheets of film.

A disc was compressed from one of the pieces of Blend #1 betweenstainless steel caul plates and shim stock of 24 mils (0.024 inch) thickfor -15 min. at 350° F.-360° F. at a pressure of 30 tons on a 6 inchdiameter ram. The platens of the molding press measured 12 inches×12inches in size.

The molded disc was removed from between the heated platens and cooledin another press under pressure for about 5 min.

The resultant disc of blended material measured approximately 10 inchesin diameter, 24 mils (0.024 inch) thick, and weighed approximately 50 g.

The disc was subsequently immersed in acetone solvent to extract thePMMA (Acrylite™ polymer) phase. The resultant composite film structureis microporous and contains the remaining unextractable polymers, thatis, PGA (85 wt. %) and fibrillated PTFE (15 wt. %) binder.

EXAMPLE 9

The following tricomponent blend is prepared similarly to Example 8.

A microporous fibrillated PTFE containing PEVA and high levels ofmicropulverized PGA polymer is blended on a rubber mill pre-heated to˜160-170° C. The composition of the blend is as follows:

    ______________________________________                                        Blend                                                                         No.     Components             Wt. q.                                         ______________________________________                                        2       Acrylite ™ H-12 Compound                                                                          200                                                    PTFE (DuPont 30B susp.)                                                                              30                                                     Poly(ethylene-Vinyl Acetate), (PEVA)                                                                 30                                                     PGA (micropulv.)       140                                            ______________________________________                                    

The blend was removed from the rubber mill in one uniform sheet. Whilethe blended sheet was still hot from the mill, it was cut into 8approximately equal parts to be used for pressing into thinner sheets offilm.

A disc was compressed from one of the pieces of Blend #2 betweenStainless Steel (SS) caul plates and shim stock of 24 mils. thick. Adisc was formed which measured approximately 10.5" diameter and 24 milsthick (0.024") and weighed 49 g.

After extracting the PMMA (Acrylite™) polymer phase with solvent, theresultant microporous film structure is a composite of the remainingunextractable polymer components namely, PGA (70 wt. %), PEVA (I5 wt.%), and fibrillar PTFE (15%).

EXAMPLE 10

A micropulverized PGA polymer biocomponent blend, Example 9, is blendedon a rubber mill pre-heated ˜160°-70° C. The composition of the blend isas follows:

    ______________________________________                                        Blend No.                                                                              Components         Wt. q.                                            ______________________________________                                        3        Acrylite ™ H-12 Compound                                                                      200                                                        PTFE (30B susp.)   10     (12 ml.)                                            PGA (micropulv.)   190                                               ______________________________________                                    

The blend was removed from the rubber mill in one uniform sheet. Whilethe blended sheet was still hot from the mill, it was cut into 8approximately equal parts to be used for pressing into thinner sheets offilm.

One plaque from blend #3 above was compressed between stainless steelcaul plates and shim stock (44 mil. or 0.044") for about 15 min. at350-360° F. at a pressure of tons on a 6" diameter ram. The platensmeasured 12×12". They were removed and cooled under pressure for about 5min. A disc was formed which measured approximately 7.5 inches diameterand approximately 43 mils thick (0.043") weighing 52 g.

After extruding the PMMA (Acrylite™) polymer phase with solvent, theresultant microporous film structure is a PGA (95 wt. %), and fibrillarPTFE (5 wt %).

EXAMPLE 11

The density of sheets compressed to a thickness of mils (0.024") fromthe blends in Examples 8 to 10 are as follows:

    ______________________________________                                        Example 8      Sheet #1     1.28 g/cc                                                        Sheet #2     1.33 g/cc                                         Example 9      Sheet #1     1.26 g/cc                                                        Sheet #2     1.26 g/cc                                         Example 10     Sheet #1     1.32 g/cc                                                        Sheet #2     1.32 g/cc                                         ______________________________________                                    

The above sheets were extracted by immersing them four times in acetone,at 16 hours each, replacing the acetone after each 16 hour immersionwith clean fresh acetone. The sheets were then washed in methanol,pressed between blotter paper, and air dried.

EXAMPLE 12

The following is the PMMA extraction data for the sheets of Examples 8to 10.

    ______________________________________                                                 Weight After                                                                           Weight Before                                                        Acetone  Acetone     % PMMA                                                   Extraction                                                                             Extraction  Extracted                                       ______________________________________                                        Example 8:                                                                             #1    30.34 g.   61.82 g.  49.07                                              #2    21.71 g.   43.01 g.  50.47                                     Example 9:                                                                             #1    23.32 g.   47.2 g.   49.4                                               #2    23.68 g.   47.9 g.   49.44                                     Example 10:                                                                            #1    25.99 g.   53.2 g.   48.9                                               #2    27.67 g.   56.4 g.   49.06                                     ______________________________________                                    

EXAMPLE 13

Sheets #2 from Example above were cut into pieces measuring 1/2 inch ×1inch and were sterilized with ethylene oxide gas in preparation foranimal implant testing.

Samples of these three types of microporous composite membranestructures were evaluated for material integrity, adsorption, and tissuereaction when implanted subcutaneously in rabbits for up to 6 months.

Two samples of each membrane were implanted subcutaneously on each sideof the abdominal midline in each of five adult New Zealand albinorabbits. Test intervals were scheduled for 14 days, 1, 2, 3 and 6months. The rabbit scheduled for six months received only one of theExample 11 samples.

At the end of the test interval one sample from each membranecomposition was resected en bloc and prepared for microscopicexamination. The other sample was removed and subjected to manualmanipulation to determine its consistency.

Results

Morbidity and Mortality

Four of the animals were healthy at term. One animal developed ulceratedfoot and heel pads and was sacrificed at 65 days instead of thescheduled 3 months. This problem was not associated with the implantmaterials.

Summary and Conclusions

Initially, all three membrane types were pliable and resistant tostretch. By 14 days and thereafter the bicomponent materials werepliable but "taffy" like. The tricomponent membrane maintained itsintegrity throughout the study. No adverse gross tissue response norgross evidence of absorption was seen at any interval.

Microscopically the membranes stimulated a slight to moderate phagocyticresponse and thin fibrous capsule formation. The least response was seenwith the tricomponent membrane. Material degradation appears to be duemore to phagocytosis than to hydrolysis.

Due to the material integrity and lack of tissue reaction seen with the15% PTFE/15% PEVA/70% PGA membranes, this material is preferred.Possible uses for the material are as a soft tissue patch and/or asegmental replacement of a hollow organ. This material, either alone orin combination with other absorbable (e.g., GLY/TMC) and/ornonabsorbable (e.g., a polybutester) materials, may also be useful toprevent or reduce tissue adhesions and/or as a pericardial patch.

The gross observations are shown in Table 1.

                                      TABLE 1                                     __________________________________________________________________________    Tissue Reaction         Consistency                                                 14 30    59 65 184                                                                              14    30   59    65    184                            Sample ID                                                                           Days                                                                             Days  Days                                                                             Days                                                                             Days                                                                             Days  Days Days  Days  Days                           __________________________________________________________________________    Example 9                                                                           none                                                                             none  none                                                                             none                                                                             none                                                                             stretchy                                                                            same same  same  same                                                   "taffy-like"                                                                  pliable                                               Example 10                                                                          none                                                                             none  none                                                                             none                                                                             none                                                                             no stretch                                                                          same same  same  same                                                   pliable                                                                       strong                                                Example 11                                                                          none                                                                             slight                                                                              none                                                                             none                                                                             none                                                                             no stretch                                                                          stretchy                                                                           stretchy                                                                            very  same                                    neovascu-      pliable                                                                             pliable                                                                            "taffy-like"                                                                        "taffy-like"                                  larity         fibrous on weak                                                               breaking                                              __________________________________________________________________________

I claim:
 1. A composite material for use with mammalian tissueconsisting essentially of:(a) an unsintered, microfibrillar,non-absorbable biocompatible component prepared frompolytetrafluoroethylene, (b) a particulate bioabsorbale fillermanufactured from a polymer prepared from one or more monomers selectedfrom the group consisting of lactides, carbonates, oxalates andlactones, and (c) a non-absorbable, biocompatible thermoplasticcomponent manufactured from a polymer which is liquid at a temperaturefrom about 150° to 200° C. and solid at ambient temperature, and whichprovides additional integrity to the unsintered component.
 2. Thematerial of claim 1 wherein the particulate bioabsorbable filler isselected from the group consisting of lactides, carbonates and lactones.3. The material of claim 2 wherein the lactides are selected from thegroup consisting of glycolide and 3,6-dimethyl-1,4-dioxan-2,5-dione; thecarbonate is 1,3-dioxan-2-one; and the lactones are selected from thegroup consisting of e-caprolactone and 1,4-dioxan-2-one.
 4. The materialof claim 3 wherein the particulates, bioabsorbable filler ismanufactured from glycolide.
 5. A composite material for use withmammalian tissue comprising a first part consisting of the compositematerial of claim 1 in the form of a sheet, the sheet having two sides;and a second part affixed to at least one side of said sheet, the secondpart comprising a bioabsorbable textile reinforcement component, thebioabsorbable reinforcement component being woven or knitted, andmanufactured from the same or a different polymer then the particulatebioabsorable filler of the first part.
 6. The material of claim 5wherein the bioabsorable textile reinforcement component is selectedfrom the group consisting of lactides, carbonates and lactones.
 7. Thematerial of claim 6 wherein the lactides are selected from the groupconsisting of glycolide and 3,6-dimethyl-1,4-dioxan-2,5-dione; thecarbonate is 1,3-dioxan-2-one; and the lactones are selected from thegroup consisting of e-caprolactone and 1,4-dioxan-2-one.
 8. The materialof claim 7 wherein said bioabsorable textile reinforcement material isaffixed to both sides of the first part.
 9. The material of claim 8wherein said bioabsorable textile reinforcement component is laminatedto said first part.
 10. The material of claims 1 or 2 or 3 or 4 whereinthe non-absorbable, thermoplastic component is poly(ethylene-vinylacetate).
 11. A composite material for use with mammalian tissueconsisting essentially of:(a) an unsintered, microfibrillar,non-absorbable biocompatible component prepared frompolytetrafluoroethylene, (b) a micropulverized bioabsorbable powdermanufactured from a polymer prepared from one or more monomers selectedfrom the group consisting of lactides, carbonates, oxalates andlactones, and (c) a non-absorbable, biocompatible thermoplasticcomponent manufactured from a polymer which is liquid at a temperaturefrom about 150° to 200° C. and solid at ambient temperature, and whichprovides additional integrity to the unsintered component.
 12. Acomposite material for use with mammalian tissue consisting essentiallyof:(a) an unsintered, microfibrillar, non-absorbable biocompatiblecomponent prepared from polytetrafluoroethylene, and (b) a bioabsorbablepowder manufactured from a polymer prepared from one or more monomersselected from the group consisting of lactides, carbonates, oxalates andlactones, and optionally (c) a non-absorbable, biocompatiblethermoplastic component manufactured from a polymer which is liquid at atemperature from about 150° to 200° C. and solid at ambienttemperatures, and which provides additional integrity to the unsinteredcomponent.
 13. The material of claim 11 wherein the composite materialis in the form of a sheet.
 14. The material of claim 11 wherein thecomposite material is in the form of a hollow tube.
 15. The material ofclaim 7 wherein the non-absorbable thermoplastic component ispoly(ethylene-vinyl acetate).
 16. The material of claim 13 wherein saidnon-absorbable, thermoplastic component is poly(ethylene-vinyl acetate).17. A composite material for use with mammalian tissue comprising afirst part consisting of the composite material of claims 11 or 12 inthe form of a sheet, the sheet having two sides; and a second partaffixed to at least one side of said sheet, the second part comprising abioabsorbable textile reinforcement component, the bioabsorbable textilereinforcement component being woven or knitted, and manufactured fromthe same or a different polymer than the bioabsorable powder of thefirst part.
 18. The material of claim 17 wherein the bioabsorable powderand textile reinforcement component are selected from the groupconsisting of lactides, carbonates and lactones.
 19. The material ofclaim 18 wherein the lactides are selected from the group consisting ofglycolide and 3,6-dimethyl-1,4-dioxan-2,5-dione; the carbonate is1,3-dioxan-2-one; and the lactones are selected from the groupconsisting of ε-caprolactone and 1,4-dioxane-2-one.
 20. The material ofclaim 18 wherein the textile reinforcement component is affixed to bothsides of the first part.